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Microsomal incubation studies revealed that oxidative metabolism is very rapid with this compound
crosses the blood brain barrier and then results in increase in brain O-GlcNAc levels in a dose- and time-dependent manner
InChi: InChI=1S/C36H56O6/c1-21(2)22-12-17-36(30(40)41)19-18-34(8)23(28(22)36)10-11-25-33(7)15-14-26(42-27(37)20-31(3
Chemical Name: benzyl(2-chloroethyl)(1-phenoxypropan-2-yl)amine hydrochloride
Identification of Potent and Selective Thyroid Stimulating Hormone Receptor Agonists
Gepotidacin S enantiomer Catalog No.:M15838-C Microsomal incubation studies revealed thatGepotidacin S enantiomer is an S enantionmer of gepotidacin. Product information CAS Number: 2319789 82 5 Molecular Weight: 448. 52 Formula: C24H28N6O3 Chemical Name: (3S) 3 ({4 [({2H,3H,4H pyrano[2,3 c]pyridin 6 yl}methyl)amino]piperidin 1 yl}methyl) 1,4,7 triazatricyclo[6. 3. 1. 0,]dodeca 6,8(12),9 triene 5,11 dione Smiles: O=C1C=CC2N=CC(=O)N3[C@@H](CN4CCC(CC4)NCC4=CC5CCCOC=5C=N4)CN1C3=2 InChiKey: PZFAZQUREQIODZ IBGZPJMESA N InChi: InChI=1S